4.7 Review

New Carbapenemase Inhibitors: Clearing the Way for the β-Lactams

Journal

Publisher

MDPI
DOI: 10.3390/ijms21239308

Keywords

carbapenemase; inhibitor; antibiotic resistance; carbapenem resistance; metallo-β -lactamases; serine-β -lactamases

Funding

  1. National Plan for Scientific Research, Development and Technological Innovation 2013-2016 [PI15/00860, PI18/00501, PI17/01482, PI20/1212]
  2. ISCIII-General Subdirection of Assessment and Promotion of the Research-European Regional Development Fund (FEDER) A way of making Europe
  3. GAIN-Agencia Gallega de Innovacion-Conselleria de Economia, Emprego e Industria [IN607A 2016/22]
  4. Planes Nacionales de I + D + i 2008-2011/2013-2016
  5. Instituto de Salud Carlos III, Subdireccion General de Redes y Centros de Investigacion Cooperativa, Ministerio de Economia y Competitividad, Spanish Network for Research in Infectious Diseases - European Development Regional Fund A way to achieve Europe [REIPI RD16/0016/006]
  6. operative program Intelligent Growth 2014-2020
  7. Rio Hortega program (ISCIII) [CM19/00219]
  8. pFIS program (ISCIII) [PI17/01482]

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Carbapenem resistance is a major global health problem that seriously compromises the treatment of infections caused by nosocomial pathogens. Resistance to carbapenems mainly occurs via the production of carbapenemases, such as VIM, IMP, NDM, KPC and OXA, among others. Preclinical and clinical trials are currently underway to test a new generation of promising inhibitors, together with the recently approved avibactam, relebactam and vaborbactam. This review summarizes the main, most promising carbapenemase inhibitors synthesized to date, as well as their spectrum of activity and current stage of development. We particularly focus on beta-lactam/beta-lactamase inhibitor combinations that could potentially be used to treat infections caused by carbapenemase-producer pathogens of critical priority. The emergence of these new combinations represents a step forward in the fight against antimicrobial resistance, especially in regard to metallo-beta-lactamases and carbapenem-hydrolysing class D beta-lactamases, not currently inhibited by any clinically approved inhibitor.

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